RecallHawk
Class II Recall

Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC

Saint Francis Apizza LLC

Summary

The FDA issued a Class II for Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged in by Saint Francis Apizza LLC. Reason: Undeclared soy allergen: soybean oil and soy lecithin.

Details

Source

Food Recall

External ID

H-0022-2027

Action Date

2026-10-14

Status

Ongoing

Category

food

Product Description

Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27759 1

Lot/Code Info: Best By: all dates through 3/30/2027

Quantity Affected: 4,255 individual units

Reason for Recall

Undeclared soy allergen: soybean oil and soy lecithin

Distribution

KY, OH

Type: Voluntary: Firm initiated

Recall Initiated: 2026-10-01

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.

Saint Francis Apizza LLC has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Saint Francis Apizza LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Saint Francis Apizza LLC have FDA actions?

Saint Francis Apizza LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0022-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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